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Constantin G. Daniliuc

Researcher Next ID · RN-032011

Researcher · Chemistry

University of Münster

Münster, Germany

Accepting doctoral researchersFunding unknown
Works count
3,369
Citation count
31,125
H-index
87
i10-index
601

Research interests

Chemistry
Materials Science
Crystallization and Solubility Studies
X-ray Diffraction in Crystallography
Organoboron and organosilicon chemistry
Crystallography and molecular interactions
Catalytic C–H Functionalization Methods

Publications

  • Lewis Acid Catalyzed Formal (3+2)‐Cycloaddition of Bicyclo[1.1.0]butanes with Ketenes

    Angewandte Chemie International Edition · 2023 · 10.1002/anie.202304771

  • Dearomative ring expansion of thiophenes by bicyclobutane insertion

    Science · 2023 · 10.1126/science.adh9737

  • Catalytic Formal [2π+2σ] Cycloaddition of Aldehydes with Bicyclobutanes: Expedient Access to Polysubstituted 2‐Oxabicyclo[2.1.1]hexanes

    Angewandte Chemie International Edition · 2023 · 10.1002/anie.202305043

  • ortho -Selective Dearomative [2π + 2σ] Photocycloadditions of Bicyclic Aza-Arenes

    Journal of the American Chemical Society · 2023 · 10.1021/jacs.3c02961

  • Synthesis of Polysubstituted 2-Oxabicyclo[2.1.1]hexanes via Visible-Light-Induced Energy Transfer

    Journal of the American Chemical Society · 2022 · 10.1021/jacs.2c09248

  • Intermolecular [2π+2σ]-photocycloaddition enabled by triplet energy transfer

    Nature · 2022 · https://doi.org/10.1038/s41586-022-04636-x

  • Photochemical single-step synthesis of β-amino acid derivatives from alkenes and (hetero)arenes

    Nature Chemistry · 2022 · 10.1038/s41557-022-01008-w

  • Photochemical intermolecular dearomative cycloaddition of bicyclic azaarenes with alkenes

    Science · 2021 · https://doi.org/10.1126/science.abg0720

  • Metal-free photosensitized oxyimination of unactivated alkenes with bifunctional oxime carbonates

    Nature Catalysis · 2021 · 10.1038/s41929-020-00553-2

  • Boron-enabled geometric isomerization of alkenes via selective energy-transfer catalysis

    Science · 2020 · 10.1126/science.abb7235

  • Diastereodivergent synthesis of enantioenriched α,β-disubstituted γ-butyrolactones via cooperative N-heterocyclic carbene and Ir catalysis

    Nature Catalysis · 2019 · 10.1038/s41929-019-0387-3

  • Discovery of Unforeseen Energy-Transfer-Based Transformations Using a Combined Screening Approach

    Chem · 2019 · https://doi.org/10.1016/j.chempr.2019.06.004

  • Highly Enantioselective [5 + 2] Annulations through Cooperative N-Heterocyclic Carbene (NHC) Organocatalysis and Palladium Catalysis

    Journal of the American Chemical Society · 2018 · 10.1021/jacs.8b00868

  • Mechanistic Studies on a Cooperative NHC Organocatalysis/Palladium Catalysis System: Uncovering Significant Lessons for Mixed Chiral Pd(NHC)(PR3) Catalyst Design

    Journal of the American Chemical Society · 2017 · 10.1021/jacs.7b00462

  • General Enantioselective C−H Activation with Efficiently Tunable Cyclopentadienyl Ligands

    Angewandte Chemie International Edition · 2017 · https://doi.org/10.1002/anie.201611981

  • Redox‐Neutral Manganese(I)‐Catalyzed C−H Activation: Traceless Directing Group Enabled Regioselective Annulation

    Angewandte Chemie International Edition · 2017 · 10.1002/anie.201707396

  • Cooperative N-Heterocyclic Carbene/Palladium-Catalyzed Enantioselective Umpolung Annulations

    Journal of the American Chemical Society · 2016 · https://doi.org/10.1021/jacs.6b04364

  • Unnatural Amino Acid Synthesis Enabled by the Regioselective Cobalt(III)‐Catalyzed Intermolecular Carboamination of Alkenes

    Angewandte Chemie International Edition · 2016 · 10.1002/anie.201608729

  • Switchable selectivity in an NHC-catalysed dearomatizing annulation reaction

    Nature Chemistry · 2015 · 10.1038/nchem.2337

  • N‐Heterocyclic Carbene Catalyzed Formal [3+2] Annulation Reaction of Enals: An Efficient Enantioselective Access to Spiro‐Heterocycles

    Angewandte Chemie International Edition · 2014 · 10.1002/anie.201405381

  • N-Heterocyclic Carbene Catalyzed Switchable Reactions of Enals with Azoalkenes: Formal [4 + 3] and [4 + 1] Annulations for the Synthesis of 1,2-Diazepines and Pyrazoles

    Journal of the American Chemical Society · 2014 · 10.1021/ja510737n

  • The CH Activation/1,3‐Diyne Strategy: Highly Selective Direct Synthesis of Diverse Bisheterocycles by Rh III Catalysis

    Angewandte Chemie International Edition · 2014 · 10.1002/anie.201403782

  • N -Aminopyridinium Salts as Precursors for N-Centered Radicals – Direct Amidation of Arenes and Heteroarenes

    Organic Letters · 2014 · https://doi.org/10.1021/ol503338b

  • Stereospecific Formal [3+2] Dipolar Cycloaddition of Cyclopropanes with Nitrosoarenes: An Approach to Isoxazolidines

    Angewandte Chemie International Edition · 2014 · 10.1002/anie.201400885

  • 6‐Trifluoromethyl‐Phenanthridines through Radical Trifluoromethylation of Isonitriles

    Angewandte Chemie International Edition · 2013 · https://doi.org/10.1002/anie.201306082

  • 6-Phosphorylated Phenanthridines from 2-Isocyanobiphenyls via Radical C–P and C–C Bond Formation

    Organic Letters · 2013 · 10.1021/ol403256e

Current projects

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